3-ALPHA,11-BETA-DIHYDROXY-17A-OXA-D-HOMO-5-ALPHA-ANDROSTAN-17-ONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | IEZpWmuRoDN |
|---|---|
| InChI | InChI=1S/C19H30O4/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)23-19(14,2)10-15(21)17(13)18/h11-15,17,20-21H,3-10H2,1-2H3/t11-,12+,13-,14-,15-,17+,18-,19-/m0/s1 |
| InChIKey | KINLJDMAUPWNHF-PTXZMSDUSA-N |
| Mol Weight | 322.45 g/mol |
| Molecular Formula | C19H30O4 |
| Exact Mass | 322.214409 g/mol |
| Enantiomer InChIKey | KINLJDMAUPWNHF-RWTSLDOESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
5α-Androstan-3α,11β-diol-17-one
5α-Androstan-3β,11β-diol-17-one
5β-pregnane-3α,11β,20α,21-tetrol
Androstane-3,11,17-triol, 3,17-diformate, (3.alpha.,5.beta.,11.beta.,17.beta.)-
(17-formyloxy-11-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl) formate
Cholestane-3,11-diol
3α,11β,21,21-tetrahydroxy-5β-pregnan-20-one
5.ALPHA.-ANDROSTANE-3.BETA.,11.ALPHA.,16.BETA.-TRIOL-TRI-TRIMETHYLSILYL ETHER
[(1S,2R,3S,5S,8R,9S,10S,13S,14S,17S)-1,2-dideuterio-10,13-dimethyl-3-trimethylsilyloxy-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]oxy-trimethyl-silane
| Title | Journal or Book | Year |
|---|---|---|
| Transformation of some 3α-substituted steroids by Aspergillus tamarii KITA reveals stereochemical restriction of steroid binding orientation in the minor hydroxylation pathway | The Journal of Steroid Biochemistry and Molecular Biology | 2010 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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